Minature Derf Needle Holder 132-376

by Sontec Instruments, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00192896022195 UDI-DI	Date4 Oct 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Minature Derf Needle Holder
Generic Name: Suturing needle holder, reusable
Model / Ref / Catalog: 132-376

Primary DI / UDI-DI: 00192896022195
FDA Product Code: FHQ
GMDN Term: Suturing needle holder, reusable

Device Class: Class I
Regulation Number: 876.4730
GUDID distribution status: In Commercial Distribution

Size: Length — 3.5 Inch

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Properties

Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No